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临床试验/NCT03620266
NCT03620266进行中(未招募)不适用

Effects of Bilberry and Oat Intake on Plasma Lipid Profile, Inflammation, and Exercise Capacity in Patients With Type 2 Diabetes and/or Myocardial Infarction (BioDiaMI): a Randomized, Double-blind, Placebo-controlled Trial

Ole Frobert, MD, PhD8 个研究点 分布在 2 个国家目标入组 900 人开始时间: 2021年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
900
试验地点
8
主要终点
Plasma levels of LDL cholesterol

研究概览

简要总结

Background:

Bilberries from Sweden, rich in polyphenols, have shown cholesterol-lowering effects in small studies, and the cholesterol-lowering properties of oats, with abundant beta-glucans and potentially bioactive phytochemicals, are well established. Both may provide cardiometabolic benefits for patients with manifest chronic cardiometabolic disease, such as type 2 diabets mellitus (T2DM) and myocardial infarction (MI). However, large studies of adequate statistical power and appropriate duration are needed to confirm clinically relevant treatment effects. No previous study has evaluated the potential additive or synergistic effects of bilberry combined with oats on cardiometabolic risk factors.

Design:

This is a double-blind, randomized, placebo-controlled clinical trial. Our primary objective is to assess cardioprotective effects of diet supplementation with dried bilberry and with bioprocessed oat bran, with a secondary explorative objective of assessing their combination, compared with a neutral isocaloric reference supplement, for patients diagnosed with T2DM and/or MI. Patients will be randomized 1:1:1:1 to a three-month intervention. The primary endpoint is the difference in LDL cholesterol change between the intervention groups after three months. The major secondary endpoint is exercise capacity at three months. Other secondary endpoints include plasma concentrations of biochemical markers of inflammation, glycaemia, and gut microbiota composition after three months.

Implications:

Secondary prevention after cardiometabolic disease, including T2DM and MI, has improved during the last decades but diabetes complications, readmissions and cadiovascular related deaths following these conditions remain large health care challenges. Controlling hyperlipidemia, hyperglycaemia, hypertension and inflammation is critical to preventing (new) cardiovascular events, but novel pharmacological treatments for these conditions are expensive and associated with negative side effects. If bilberry and/or oat, in addition to standard medical therapy, can lower LDL cholesterol and inflammation more than standard therapy alone, this could be a cost-effective and safe dietary strategy for secondary prevention in high-risk patients or risk prevention in subjects with T2DM.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmed T2DM diagnosis (any treatment modality accepted) and/or within 3 years post STEMI or NSTEMI
  • Completed coronary angiography/PCI
  • Male and female subjects ≥18 years
  • Allocated to atorvastatin at a daily dose of 80 mg (only eligible for patients enrolled up to 7 days post MI and not for T2D subjects)
  • Written informed consent

排除标准

  • Emergency coronary artery bypass grafting
  • <18 years of age
  • LDL cholesterol <2.0 mmol/L
  • Daily intake or the intent to initiate daily intake of bilberry in any form or daily intake of >15 g of oatmeal or equivalent
  • Food allergy/intolerance to gluten, bilberries or legumes
  • Previous randomization in the BioDiaMI trial
  • Inability to provide informed consent

结局指标

主要结局

Plasma levels of LDL cholesterol

时间窗: Three months

The effect of intervention on difference between the groups of LDL cholesterol after three months

次要结局

  • Symptom-limited bicycle ergometer test(Three months)
  • Self-reported physical activity level(Three months)
  • Urine albumin-creatinine ratio(Three months)
  • Fecal samples of gut microbiota composition(Three months)
  • Left ventricular systolic function(Three months)
  • Systolic and diastolic blood pressure(Three months)
  • Plasma lipid profile(Three months)
  • Resting heart rate(Three months)
  • Dynamic unilateral heel-lft and unilateral shoulder flexion tests(Three months)
  • Untargeted plasma metabolome(Three months)
  • Continuous glucose monitoring with Continuous Glucose Monitors (CGM) - FreeStyle model 2(Three months)
  • Plasma Cardiac Troponin Concentration(Three months)
  • Plasma NT-proBNP Concentration(Three months)
  • Plasma hs-CRP Concentration(Three months)
  • Plasma IL-6 Concentration(Three months)
  • Glycosylated Hemoglobin (HbA1c)(Three months)
  • Fasting Plasma Insulin Concentration(Three months)
  • Fasting Plasma C-Peptide Concentration(Three months)
  • Serum Creatinine Concentration(Three months)
  • Fasting Plasma Glucose Concentration(Three months)
  • Serum Cystatin C Concentration(Three months)
  • Body composition with multi-frequency bioimpedance(Three months)
  • Diabetic retinal changes(Three months)
  • Platelet aggregation (Primary hemostasis)(Three months)
  • P-selectin levels (Primary hemostasis)(Three months)
  • Ex vivo thrombin generation (Secondary hemostasis)(Three months)
  • Prothrombin fragment 1+2 (Secondary hemostasis)(Three months)
  • Fibrinolysis speed(Three months)
  • Fibrinolytic capacity(Three months)
  • Fibrinolytic markers(Three months)
  • Endothelial activation(Three months)
  • Inflammation(Three months)
  • Oxidative stress(Three months)

研究者

发起方
Ole Frobert, MD, PhD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ole Frobert, MD, PhD

Professor

Region Örebro County

研究点 (8)

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